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Dystonia Panel NGS Genetic Test

4,400 د.إ

-27%

The “Dystonia Panel NGS Genetic Test” offered by DNA Labs UAE is a comprehensive genetic screening designed to diagnose various forms of dystonia, a neurological movement disorder characterized by involuntary muscle contractions, which can result in twisting and repetitive movements or abnormal postures. Utilizing Next-Generation Sequencing (NGS) technology, this panel test can analyze multiple genes known to be associated with dystonia, providing a precise diagnosis that can aid in tailoring specific treatment plans for patients.

The test is priced at 4400 AED and is conducted in the state-of-the-art facilities of DNA Labs UAE, ensuring high-quality standards and accurate results. By identifying the genetic underpinnings of dystonia, the test not only facilitates a better understanding of the condition for the patient and their family but also opens up possibilities for targeted therapies and interventions, potentially improving the quality of life for those affected by dystonia.

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  • This test is not intended for medical diagnosis or treatment
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Dystonia Panel NGS Genetic Test

Cost: AED 4400.0

Symptoms and Diagnosis

Dystonia is a movement disorder characterized by involuntary muscle contractions and spasms. The Dystonia panel NGS genetic DNA test is a diagnostic tool used to identify mutations in genes associated with dystonia.

Test Details

The Dystonia panel NGS genetic DNA test utilizes next-generation sequencing (NGS) technology, which allows for the comprehensive analysis of multiple genes simultaneously. This test analyzes the following genes:

  1. DYT1
  2. DYT6
  3. DYT5a
  4. DYT5b
  5. DYT2
  6. DYT7
  7. DYT13
  8. DYT15
  9. DYT16
  10. DYT17
  11. DYT20
  12. THAP1

The test helps confirm a diagnosis of dystonia, identify the specific subtype of dystonia, and guide treatment decisions. It can also identify individuals at risk of developing dystonia, allowing for early intervention and management.

Pre-Test Information

Prior to the test, a genetic counseling session is conducted to gather clinical history and draw a pedigree chart of family members affected by dystonia.

Test Process

The Dystonia panel NGS genetic DNA test requires a blood or saliva sample, which is sent to the laboratory for analysis. Results are typically available within 3 to 4 weeks.

Conclusion

The Dystonia panel NGS genetic DNA test is a valuable tool in diagnosing and managing dystonia. With its ability to analyze multiple genes simultaneously, it provides comprehensive insights for healthcare providers specializing in movement disorders.

 

Test NameDystonia panel NGS Genetic DNA Test
Components 
Price4400.0 AED
Sample ConditionBlood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery3 to 4 Weeks
MethodNGS Technology
Test typeNeurological Disorders
DoctorNeurologist
Test Department:Genetics
Pre Test InformationClinical History of Patient who is going for Dystonia panel NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Dystonia panel
Test Details

The Dystonia panel NGS genetic DNA test is a diagnostic tool that is used to identify mutations in genes that are associated with dystonia, a movement disorder that causes involuntary muscle contractions and spasms. The test is performed using next-generation sequencing (NGS) technology, which allows for the rapid and comprehensive analysis of multiple genes at once.

The Dystonia panel NGS genetic DNA test analyzes a set of genes that have been implicated in the development of dystonia, including:

1. DYT1

2. DYT6

3. DYT5a

4. DYT5b

5. DYT2

6. DYT7

7. DYT13

8. DYT15

9. DYT16

10. DYT17

11. DYT20

12. THAP1

The test can help to confirm a diagnosis of dystonia, identify the specific subtype of dystonia, and guide treatment decisions. It may also be used to identify individuals who are at risk of developing dystonia, allowing for early intervention and management.

The Dystonia panel NGS genetic DNA test is typically ordered by a healthcare provider who specializes in the diagnosis and treatment of movement disorders. The test requires a blood or saliva sample, which is sent to a laboratory for analysis. Results are typically available within a few weeks.

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